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O utilizador não deve tocar simultanea-
mente no doente e na ficha de saída
doadaptadorAC.
•Esteequipamentocorrespondeànormaeuropeia
EN60601-1-2eestásujeitoamedidasdeprecauçãopar-
ticularesrelativasàcompatibilidadeelectromagnética.
Por favor, tenha em atenção que os equipamentos de
telecomunicaçõesAFportáteisemóveispodeminterferir
com este equipamento. Poderá solicitar informações mais
pormenorizadas no endereço do centro de atendimento a
clientes, indicado nestas instruções.
•OequipamentoestáconformeaDirectivaEuropeiarela-
tiva aos produtos médicos, 93/42/EC a Lei alemã relativa
aos materiais médicos e as directivas europeias
EN1060-1(medidoresdetensãoarterialnãoinvasivos
parte1:requisitosbásicos)eEN1060-3(medidoresde
tensão arterial não invasivos, parte 3: requisitos comple-
mentares para sistemas de medição de tensão arterial
electromecânicos).
•Quandooaparelhoéusadoparafinscomerciaisou
económicos, devem realizar-se testes regulares para con-
trolo da exactidão da medição de acordo com a Lei alemã
relativa aos exploradores de produtos médicos. Mesmo
quando usado para fins particulares, recomendamos que
realize, no fabricante, um controlo da exactidão da me-
dição em intervalos de dois em dois anos.
23


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